Mumbai

Thorough understanding of Quality Control investigations, including Lab Incidents, OOS, and OOT. Relevant experience in Oral Solid Dosage formulations and / or Active Pharmaceutical Ingredient processes.

PhD Biotechnology in the field of Algal Biotechnology. The upper age limit is relax-able up-to 5 years in the case of candidates belonging to scheduled castes/tribes/OBC, women and physically handicapped candidates.

Performing post-submission processing activities such as receiving acknowledgment from authority of submission receipt; capturing and the electronic receipt and metadata in RIM; communicating submission receipt to key stakeholders

Develop and maintain a comprehensive understanding of the company's products, particularly in the cardiovascular therapeutic area, while staying updated on the latest medical advancements, clinical guidelines, and treatment protocols.

Design and execute multistep organic syntheses under the supervision of senior scientists. Having knowledge of enzymatic reactions. Perform compound purification using techniques such as column chromatography, recrystallization, HPLC, etc.

Graduation or Post Graduation in Science - Preferably Pharmacy At least 5 years ideally experience in the Pharmaceutical or related industry, ideally with a mix of Manufacturing, QA operations, Distribution Warehouse management and Regulatory Affairs

Bachelors degree in Pharmacy, Bachelors of Ayurvedic medicine and surgery along with Post Graduate Diploma, Degree in Hospital Administration Management from recognised University.

Ph.D in Pharmaceutics / Pharmacology / Nanotechnology / Biotechnology with experience in nano formulations. Post doctoral Fellow; Experience in development and characterization of nano drug delivery systems, handling cell line studies and small animals desirable.

experience in Pharmaceutical, CRO or Biotech industry; clinical drug development within the pharmaceutical industry or related industry.